@prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP708116.RAeCG6v4Z_wJUR1hPD2myBzKYX0KcSeGPLQtgxncyFLK4130_head { this: np:hasAssertion dgn-np:NP708116.RAeCG6v4Z_wJUR1hPD2myBzKYX0KcSeGPLQtgxncyFLK4130_assertion; np:hasProvenance dgn-np:NP708116.RAeCG6v4Z_wJUR1hPD2myBzKYX0KcSeGPLQtgxncyFLK4130_provenance; np:hasPublicationInfo dgn-np:NP708116.RAeCG6v4Z_wJUR1hPD2myBzKYX0KcSeGPLQtgxncyFLK4130_publicationInfo; a np:Nanopublication . dgn-np:NP708116.RAeCG6v4Z_wJUR1hPD2myBzKYX0KcSeGPLQtgxncyFLK4130_assertion a np:Assertion . dgn-np:NP708116.RAeCG6v4Z_wJUR1hPD2myBzKYX0KcSeGPLQtgxncyFLK4130_provenance a np:Provenance . dgn-np:NP708116.RAeCG6v4Z_wJUR1hPD2myBzKYX0KcSeGPLQtgxncyFLK4130_publicationInfo a np:PublicationInfo . } dgn-np:NP708116.RAeCG6v4Z_wJUR1hPD2myBzKYX0KcSeGPLQtgxncyFLK4130_assertion { miriam-gene:6657 a ncit:C16612 . lld:C0032002 a ncit:C7057 . dgn-gda:DGNb9020beab04b73cb64c0338f226e1b42 sio:SIO_000628 miriam-gene:6657, lld:C0032002; a sio:SIO_001122 . } dgn-np:NP708116.RAeCG6v4Z_wJUR1hPD2myBzKYX0KcSeGPLQtgxncyFLK4130_provenance { dgn-np:NP708116.RAeCG6v4Z_wJUR1hPD2myBzKYX0KcSeGPLQtgxncyFLK4130_assertion dcterms:description "[Given the critical role of Sox2 in normal hypothalamo-pituitary development in the mouse and the anterior pituitary hypoplasia observed in most human patients with SOX2 mutations, it remains to be established whether further pituitary hormone deficiencies might evolve with time.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en; wi:evidence dgn-void:source_evidence_literature; sio:SIO_000772 miriam-pubmed:18987493; prov:wasDerivedFrom dgn-void:befree-20150227; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^xsd:date . dgn-void:source_evidence_literature a eco:ECO_0000212; rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en; rdfs:label "DisGeNET evidence - LITERATURE"@en . } dgn-np:NP708116.RAeCG6v4Z_wJUR1hPD2myBzKYX0KcSeGPLQtgxncyFLK4130_publicationInfo { this: dcterms:created "2015-08-25T14:44:47+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetv3.0rdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }